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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113602Generated: October 28, 2026

Triethylamine → tert-butyl (3S)-3-aminopiperidine-1-carboxylate

https://huagongshe.com/reaction/2113602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(R)-1-Boc-3-hydroxypiperidineHCID 1514398—
SolventDichloromethaneHCID 6344—
Producttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—

Reaction Conditions

Temperature0 °C

Reaction Steps

Methanesulfonyl chloride (9.56 mL, 124 mmol) was added dropwise over 10 minutes to a stirred solution of 1,1-dimethylethyl (3R)-3-hydroxypiperidine-1-carboxylate (20.7 g, 103 mmol) and triethylamine (21.5 mL, 154 mmol) in dichloromethane (300 mL) at 0° C. After stirring for 3 hour at 0° C., the reaction was quenched by addition of water. The organic phase was washed with brine, dried (MgSO4), filtered and evaporated in vacuo to give an oil. This was purified by flash chromatography on silica, eluting with ethyl acetate/cyclohexane (20:80 to 50:50), to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432280B2
Source datasetuspto-grants-2008_10
ORD IDord-7858c37462804c8fa89cbaf7bc52e010
Source noteuspto-grants-2008_10